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MEDIA FOR IN-VITRO DIAGNOSTIC USE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820863
510(k) Type
Traditional
Applicant
ISLE MEDIA AND STERILE PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/16/1982
Days to Decision
18 days

MEDIA FOR IN-VITRO DIAGNOSTIC USE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820863
510(k) Type
Traditional
Applicant
ISLE MEDIA AND STERILE PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/16/1982
Days to Decision
18 days